Canonical Allele Identifier: CA422374360
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1571813622
MyVariant Identifiers: chr1:g.186650007T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680875T>C , CM000663.2:g.186680875T>C GRCh38
NC_000001.10:g.186650007T>C , CM000663.1:g.186650007T>C GRCh37
NC_000001.9:g.184916630T>C NCBI36
NG_028206.2:g.4553A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-285A>G (PTGS2) ENSP00000506242.1:n.-285A>G
NR_125801.1:n.222T>C (PACERR)